Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in mice

Idiopathic pulmonary fibrosis (IPF) patients have a high risk of developing lung cancer, with few treatment options available. Pirfenidone, an antifibrotic agent approved for the treatment of IPF, has been demonstrated to suppress the TGFβ signaling and modulate the expression of immune-related gene...

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Main Authors: Wan Qin, Jun Zou, Yongbiao Huang, Chaofan Liu, Yalin Kang, Hu Han, Yang Tang, Long Li, Bo Liu, Weiheng Zhao, Xianglin Yuan
Format: Article
Language:English
Published: Taylor & Francis Group 2020-01-01
Series:OncoImmunology
Subjects:
Online Access:http://dx.doi.org/10.1080/2162402X.2020.1824631
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author Wan Qin
Jun Zou
Yongbiao Huang
Chaofan Liu
Yalin Kang
Hu Han
Yang Tang
Long Li
Bo Liu
Weiheng Zhao
Xianglin Yuan
author_facet Wan Qin
Jun Zou
Yongbiao Huang
Chaofan Liu
Yalin Kang
Hu Han
Yang Tang
Long Li
Bo Liu
Weiheng Zhao
Xianglin Yuan
author_sort Wan Qin
collection DOAJ
description Idiopathic pulmonary fibrosis (IPF) patients have a high risk of developing lung cancer, with few treatment options available. Pirfenidone, an antifibrotic agent approved for the treatment of IPF, has been demonstrated to suppress the TGFβ signaling and modulate the expression of immune-related genes. However, for lung cancer patients with comorbid IPF, whether pirfenidone has any synergetic effect with immune checkpoint inhibitors has not been investigated. In this study, we showed that pirfenidone monotherapy attenuated tumor growth with an increased T cell inflammatory signature in tumors. Co-administration of pirfenidone with PD-L1 blockades significantly delayed the tumor growth and increased survival, compared with the effect of either treatment alone. Combination therapy promoted gene expression with a unique signature associated with innate and adaptive immune response resulted in the infiltration of immune cells and optimal T cell positioning. Furthermore, we showed a great benefit of combination therapy in alleviating the pulmonary fibrosis and reducing the tumor growth in a tumor-fibrosis model. Our results collectively demonstrated that pirfenidone facilitated antitumor immunity and enhanced the efficacy of PD-L1 blockades. It may act as an adjuvant to immunotherapy in cancer treatment, particularly, in lung cancer patients with preexisting IPF.
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spelling doaj.art-fd843a04666f45679d6c8ab9ee25a4e52022-12-21T19:52:07ZengTaylor & Francis GroupOncoImmunology2162-402X2020-01-019110.1080/2162402X.2020.18246311824631Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in miceWan Qin0Jun Zou1Yongbiao Huang2Chaofan Liu3Yalin Kang4Hu Han5Yang Tang6Long Li7Bo Liu8Weiheng Zhao9Xianglin Yuan10Tongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyTongji Hospital, Huazhong University of Science and TechnologyIdiopathic pulmonary fibrosis (IPF) patients have a high risk of developing lung cancer, with few treatment options available. Pirfenidone, an antifibrotic agent approved for the treatment of IPF, has been demonstrated to suppress the TGFβ signaling and modulate the expression of immune-related genes. However, for lung cancer patients with comorbid IPF, whether pirfenidone has any synergetic effect with immune checkpoint inhibitors has not been investigated. In this study, we showed that pirfenidone monotherapy attenuated tumor growth with an increased T cell inflammatory signature in tumors. Co-administration of pirfenidone with PD-L1 blockades significantly delayed the tumor growth and increased survival, compared with the effect of either treatment alone. Combination therapy promoted gene expression with a unique signature associated with innate and adaptive immune response resulted in the infiltration of immune cells and optimal T cell positioning. Furthermore, we showed a great benefit of combination therapy in alleviating the pulmonary fibrosis and reducing the tumor growth in a tumor-fibrosis model. Our results collectively demonstrated that pirfenidone facilitated antitumor immunity and enhanced the efficacy of PD-L1 blockades. It may act as an adjuvant to immunotherapy in cancer treatment, particularly, in lung cancer patients with preexisting IPF.http://dx.doi.org/10.1080/2162402X.2020.1824631lung canceridiopathic pulmonary fibrosispd-l1 blockadesimmune-checkpoint inhibitorspirfenidone
spellingShingle Wan Qin
Jun Zou
Yongbiao Huang
Chaofan Liu
Yalin Kang
Hu Han
Yang Tang
Long Li
Bo Liu
Weiheng Zhao
Xianglin Yuan
Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in mice
OncoImmunology
lung cancer
idiopathic pulmonary fibrosis
pd-l1 blockades
immune-checkpoint inhibitors
pirfenidone
title Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in mice
title_full Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in mice
title_fullStr Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in mice
title_full_unstemmed Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in mice
title_short Pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of PD-L1 blockade in mice
title_sort pirfenidone facilitates immune infiltration and enhances the antitumor efficacy of pd l1 blockade in mice
topic lung cancer
idiopathic pulmonary fibrosis
pd-l1 blockades
immune-checkpoint inhibitors
pirfenidone
url http://dx.doi.org/10.1080/2162402X.2020.1824631
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